An Antiferromagnetic Molecular Metal Based on a New Bent-Donor

of heat capacity, and the H-dependence of Δρ⊥/ρ⊥ up to H = 14 T at T = 0.45 K. This material is available free of charge via the Internet a...
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An Antiferromagnetic Molecular Metal Based on a New Bent-Donor Molecule Xunwen Xiao,†,§ Toshiki Hayashi,†,‡ Hideki Fujiwara,†,§ Toyonari Sugimoto,*,†,§, Satoru Noguchi,|,§ Yufeng Weng,⊥ Harukazu Yoshino,⊥ Keizo Murata,*,⊥ and Hiroko Aruga Katori# Department of Chemistry, Osaka Prefecture UniVersity, Osaka 599-8570, Japan, CREST, Japan Science and Technology Agency, Saitama 332-0012, Japan, Department of Applied Chemistry and Department of Physics and Electronics, Osaka Prefecture UniVersity, Osaka 599-8531, Japan, Department of Molecular Materials Science, Osaka City UniVersity, Osaka 558-8585, Japan, and RIKEN (The Institute of Physical and Chemical Research), Saitama 351-0198, Japan Received July 1, 2007; E-mail: [email protected]; [email protected]

Spintronic devices have generated much recent interest because they can simultaneously store and manipulate data by using both the charge and spin of an electron. A functioning spintronic device based on a tunneling magnetoresistance effect has been built in a heterojunction structure, composed of a crystalline MgO insulator and two thin ferromagnetic metallic layers (Fe, Co, Ni, etc.).1 The anticipated development of molecular-based spintronics is contingent on the discovery of a ferromagnetic molecular metal. A number of charge-transfer (CT) salts composed of several π donor molecules and magnetic metal anions with d or f spins have been prepared with this goal in mind. So far only four magnetic molecular conductors display metallic conductivity down to low temperatures and antiferromagnetic ordering of localized d spins of the magnetic FeCl4- or FeBr4- ions by significant π-d interaction with the conducting π electrons: κ-[bis(ethylenedithio)tetraselenafulvalene, BETS]2‚FeCl4,2 κ-(BETS)2‚FeBr4,3 (ethylenedioxytetrathiafulvalenoquinone-1,3-dithiolemethide, EDO-TTFVO)2‚ FeCl44 and (ethylenedithiodiselenadithiafulvalenothioquinone-1,3diselenolemethide, EDT-DSDTFVSDS)2‚FeBr4.5 While the antiferromagnetic ordering temperature has increased in the new magnetic molecular conductors, the highest temperature remains near 3 K. However, the required ferromagnetic ordering has not yet been achieved, although a molecular metal of [bis(ethylenedithio)tetrathiafulvalene]2‚[MnCr(C2O4)3] exhibited ferromagnetic order with a very weak π-d interaction.6 This situation prompts us to investigate a new donor molecule, ethylenedioxytetrathiafulvalenoquinone-1,3diselenolemethide (EDO-TTFVODS, 1), which offers two key advantages: an ethylenedioxy group that stabilizes the metallic conductivity in (EDO-TTFVO)2‚FeCl44, and a 1,3-diselenole group contributing to a strong π-d interaction between the conducting π electrons and the localized d spins in (EDT-DSDTFVSDS)2‚FeBr4.5 In this Communication we report the synthesis of a 2:1 CT salt of 1 with an FeBr4- ion, which exhibited a metallic conductivity down to 0.45 K and an antiferromagnetic ordering at the highest temperature (4.5 K) obtained so far in antiferromagnetic molecular metals.

The 1 molecule was prepared using the procedure described previously.4 The redox potentials of 1 measured in benzonitrile at † Department of Chemistry, Osaka Prefecture University. § CREST, Japan Science and Technology Agency. ‡ Department of Applied Chemistry, Osaka Prefecture University. | Department of Physics and Electronics, Osaka Prefecture University. ⊥ Osaka City University. # RIKEN (The Institute of Physical and Chemical Research).

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Figure 1. Crystal structure projected down to the bc-plane.

0 °C were +0.61 and +0.91 V versus Ag/AgCl, almost the same as those of EDO-TTFVO (+0.60 and +0.89 V).4 We performed electrochemical oxidation of 1 in 1,2-dichloroethane (DCE) containing a supporting electrolyte, NBu4‚FeBr4, with a constant electrical current of 0.1-0.2 µA. After several weeks, we isolated black platelike crystals with a molecular formula of 12‚FeBr4‚(DCE)1/2. The crystal structure is shown in Figure 1.7 The crystal contains 1 molecules alternating with (FeBr4- ion + DCE molecule) layers. Each donor layer has a two-dimensional β′′-type stacking motif. As seen from the diagonal and side-by-side donor arrays, there are comparatively close S‚‚‚S, S‚‚‚Se and Se‚‚‚Se contacts. In each anion layer two FeBr4- ions and one DCE molecule are alternately arranged along the intercolumnar direction, while the intracolumnar direction has a regular arrangement of the FeBr4- ions. Hence the Br‚‚‚Br contacts for each pair of the FeBr4- ions have comparatively short distances of 4.03 and 4.19 Å, while the distance is long (4.55 Å) between the Br atoms of the neighboring FeBr4- ions separated by one DCE molecule. On the other hand, the Br‚‚‚Br contact distance along the intracolumnar direction is 3.74 Å, which is shorter than the van der Waals distance (3.90 Å). There are also close contacts between the Se atoms of the donor molecule and the Br atoms of the FeBr4- ion. With the X-ray structure data described above, we calculated the band structure of the 1 molecule layer using a tight-binding method based on an extended Hu¨ckel approximation. The overlap integrals suggest that there are two different overlaps (b1 ) -10.6 × 10-3; b2 ) -5.15 × 10-3) in the side-by-side direction. We also find six relatively large overlap integrals along the diagonal stacking (p1 ) -11.1 × 10-3; p2 ) -3.28 × 10-3; p3 ) -2.63 × 10-3; q1 ) -9.79 × 10-3; q2 ) -2.41 × 10-3; q3 ) -3.36 × 10-3), indicating a two-dimensional interaction in the conducting ab-plane. The calculated Fermi surface is two-dimensional, but opens along the ka and kc directions because of the low symmetry of the space group (P1h). As a result, a rectangular electron pocket surrounds the C point, while two different elliptic hole pockets surround the X and Y points, respectively (Figure 2a). We measured the electrical resistance (F) of the single crystal by a four-probe method. The F values in the ab-plane (F|) and in 10.1021/ja074840q CCC: $37.00 © 2007 American Chemical Society

COMMUNICATIONS

Figure 2. (a) Fermi surface and (b) T-dependence of F| between 0.45 and 300 K (below 7 K in the inset).

Figure 3. (a) T-dependence of χp along H|a, H|b, and H|c* below T ) 15 K and (b) magnetoresistance (∆F|/F|) with H applied perpendicular to the conducting ab-plane.

the c*-direction, perpendicular to the plane (F⊥), are ca. 1 × 10-1 and 20 Ω cm at 300 K, respectively. As shown by the temperaturedependence of F| in Figure 2b, metallic behavior persists down to 0.45 K in spite of a very slight upturn in F| below 5 K. We observe a similar trend in the F⊥-T measurement. The slight increase of the F| and F⊥ values as the temperature decreases below ca. 4 K is most likely caused by the π-d interaction. We carried out SQUID measurements on the polycrystalline sample under a magnetic field H ) 1 kOe at temperatures between 1.9 and 300 K. The temperature-dependence of the paramagnetic susceptibility (χp) obeys a Curie-Weiss law [χp ) C/(T - Θ), where C is the Curie constant and Θ is the Weiss temperature] at high temperatures. Our fits give C ) 4.48 emu K mol-1 and Θ ) -18.7 K. Below 20 K the χp values become smaller than those predicted by the Curie-Weiss equations with the C and Θ values given above, and a peak appears near 4.5 K, suggesting antiferromagnetic ordering. We repeated the SQUID measurements using the single crystals to confirm the antiferromagnetic ordering, and to determine the ordering temperature (TN) and the easy axis of the magnetization. Figure 3a shows χp-T plots below 15 K when H ) 5 kOe is applied along the a-, b-, and c*-axes, respectively. Antiferromagnetic order appears near 4 K with an easy magnetization along the c*-axis. Heat capacity measurements provide a more accurate value of TN ) 4.5 K. This TN is considerably larger than those previously observed in antiferromagnetic molecular metals, that is, 0.45 K for κ-(BETS)2‚FeCl4,2 2.5 K for κ-(BETS)2‚FeBr4,3 3.0 K for (EDO-TTFVO)2‚FeCl44 and 3.3 K for (EDTDSDTFVSDS)2‚FeBr4.5 The order of TN in these materials is consistent with the spin exchange integrals for d-d and π-d interactions (Jdd and Jπd) obtained from molecular orbital calculations.8 The Jdd and Jπd values of the present FeBr4- salt are 1.86 and 14.5 K, respectively. This is the largest Jdd of all the antiferromagnetic molecular metals, while Jπd is comparable to that of (EDT-DSDTFVSDS)2‚FeBr4 (15.6 K), and noticeably larger than those of the others.

We investigated the magnetoresistance (MR) of F| at 0.45 K by applying a magnetic field perpendicular to the conducting ab-plane, with H ranging to 14 T. The H-dependence of ∆F|/F| [∆F| ) F|(H) - F|(0)] in Figure 3b shows a small negative MR (1-2%) for weak H, which reaches a maximum near 2 T. Above 7 T the MR becomes positive. Because the Fe(III) d spins are antiferromagnetically ordered below TN ) 4.5 K and no disorder is present in the crystal structure, we attribute this negative MR to the suppression of d spin scattering caused by spin alignment with the applied field. This result undoubtedly reflects the presence of the π-d interaction; however, the π-d interaction need not be weak because the MR is small. Large negative MRs were previously observed in our magnetic molecular conductors that were in semiconducting states with significant π-d interactions,5,9 whereas this FeBr4- salt is metallic. We have reported electron transport and magnetic measurements which demonstrate that the 12‚FeBr4‚(DCE)1/2 salt is a genuine molecular metal with stronger π-d interactions than (EDOTTFVO)2‚FeCl4. The small negative MR indicates that the metallic conduction is not strongly influenced by the localized d spins. We also observe that the antiferromagnetic ordering temperature is high compared to those of the antiferromagnetic molecular metals known so far, but lower than the large Jdd and Jπd values would suggest. This information may prove useful in the development of ferromagnetic molecular metals or semiconductors with significant π-d interactions. Acknowledgment. This work is supported in part by a Grantin-Aid for Scientific Research on Priority Areas of Molecular Conductors (No. 16038222) from the Ministry of Education, Culture, Sport, and Technology, Japan. Supporting Information Available: An X-ray crystallographic file for the crystal of 12‚FeBr4‚(DCE)1/2 in CIF format, the T-dependence of F⊥ between 0.45 and 300 K, the T-dependence of heat capacity, and the H-dependence of ∆F⊥/F⊥ up to H ) 14 T at T ) 0.45 K. This material is available free of charge via the Internet at http://pubs.acs.org. References (1) (a) Julliere, M. Phys. Lett. A 1975, 54A, 225-226. (b) Miyazaki, T.; Tezuka, N. J. Magn. Magn. Mater. 1995, 139, L231-L234. (c) Yuasa, S.; Nagahama, T.; Fukushima, A.; Suzuki, Y.; Ando, K. Nat. Mater. 2004, 3, 868-871. (2) Ojima, E.; Fujiwara, H.; Kato, K.; Kobayashi, H.; Tanaka, H.; Kobayashi, A.; Tokumoto, M.; Cassoux, P. J. Am. Chem. Soc. 1999, 121, 55815582. (3) Otsuka, T.; Kobayashi, A.; Miyamoto, Y.; Kikuchi, J.; Wada, N.; Ojima, E.; Fujiwara, H.; Kobayashi, H. Chem. Lett. 2000, 732-733. (4) Fujiwara, H.; Wada, K.; Hiraoka, T.; Hayashi, T.; Sugimoto, T.; Nakazumi, H.; Yokogawa, K.; Teramura, M.; Yasuzuka, S,; Murata, K.; Mori, T. J. Am. Chem. Soc. 2005, 127, 14166-14167. (5) Hayashi, T.; Xiao, X.; Fujiwara, H.; Sugimoto, T.; Nakazumi, H.; Noguchi, S.; Fujimoto, T.; Yasuzuka, S.; Yoshino, H.; Murata, K.; Mori, T.; ArugaKatori, H. J. Am. Chem. Soc. 2006, 128, 11746-11747. (6) Coronado, E.; Gala´n-Mascaro´s, J. R.; Go´mez-Garcia, C. J.; Laukhin, V. Nature 2000, 408, 447-449. (7) Crystal data for 12‚FeBr4‚(DCE)1/2: C23H14ClBr4FeO6S8Se4, Mr ) 1369.60, triclinic, a ) 7.0064(9), b ) 13.373(1), and c ) 21.334(1) Å, R ) 107.146(3), β ) 98.682(4), γ ) 92.615(5)°, V ) 1879.5(4) Å3, T ) 296 K, space group P1h, Z ) 2, µ(Mo KR) ) 9.093 cm-1, 16592 reflections measured (Rint ) 0.104), 8296 unique, of which 3765 were used in all calculations [F2 > 2.0σ(F2)]. The final R and Rw were 0.097 and 0.106, respectively. (8) Mori, T.; Katsuhara, M. J. Phys. Soc. Jpn. 2002, 71, 826-844. (9) Fujiwara, H.; Hayashi, T.; Sugimoto, T.; Nakazumi, H.; Noguchi, S.; Li, L.; Yokogawa, K.; Yasuzuka, S.; Murata, K.: Mori, T. Inorg. Chem. 2006, 45, 5712-5714.

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